1. Interchromosomal DNA-containing fibres in human cells

   • Sissel Myhra
   • Anton Brøgger

   Original Investigations Pages: 183 - 189

2. Chromosomal damage in chronic alcohol users

   • Günter Obe
   • Jan Herha

   Original Investigations Pages: 191 - 200

3. The rate of sister chromatid exchanges parallel to spontaneous chromosome breakage in Fanconi's anemia and to trenimon-induced aberrations in human lymphocytes and fibroblasts

   • K. Hayashi
   • W. Schmid

   Original Investigations Pages: 201 - 206

4. Familial translocation t(3p-;21q+) associated with both Down's and Sturge-Weber's syndrome in unbalanced state

   • Manfred Habedank
   • Gerlinde Kampe

   Original Investigations Pages: 207 - 216

5. Power of assaying inbreeding through sampling of phenotypes and mating types

   • Ranajit Chakraborty

   Original Investigations Pages: 217 - 222

6. Structural rearrangements associated with the Ph¹ chromosome in chronic granulocytic leukaemia

   • A. M. Potter
   • J. C. Sharp
   • R. J. Sokol

   Short Communications Pages: 223 - 228

7. Identification of interspecific translocation chromosomes in human-Chinese hamster hybrid cells

   • Wim Burgerhout

   Short Communications Pages: 229 - 231

8. Partial trisomy 9q: A new syndrome

   • Catherine Turleau
   • J. de Grouchy
   • P. Borniche

   Short Communications Pages: 233 - 241

9. Prenatal diagnosis of trisomy 9

   • Uta Francke
   • Kurt Benirschke
   • Oliver W. Jones

   Short Communications Pages: 243 - 250

10. Red cell esterase-D polymorphism in the population of Tuscany

    • Marino Bargagna
    • Ranieri Domenici
    • Agorasti Morali

    Short Communications Pages: 251 - 253

11. Red cell uridine monophosphate kinase polymorphism in Japanese

    • Shoji Harada
    • Masataka Itoh
    • Shogo Misawa

    Short Communications Pages: 255 - 257

12. Missing Y chromosome in juvenile chronic myelogenous leukemia

    • Taru Hays
    • James R. Humbert
    • Charles S. August

    Clinical Case Reports Pages: 259 - 264